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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665869Generated: October 31, 2026

Dichloromethane → HCID 59343387, compound

https://huagongshe.com/reaction/1665869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
Reactant(R)-2-amino-1-((S)-2,5-dihydrofuran-2-yl)ethanolHCID 55281149—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59343387HCID 5934338780%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium carbonate (12.26 g, 115.7 mmol) in water (80 mL) was added whilst stirring to a solution of (R)-2-amino-1-((S)-2,5-dihydrofuran-2-yl)ethanol (assumed to be 55 mmol) in tetrahydrofuran (100 mL). The mixture was cooled to 0° C. then benzylchloroformate (9.69 mL, 68.87 mmol) was added. The mixture was stirred at 0° C. for 45 minutes, then dichloromethane (400 mL) and water (400 mL) added. The organic phase was separated and the aqueous reextracted with dichloromethane (2×400 mL). The organic layer was washed with brine (400 mL), then dried (Na2SO4), filtered and reduced in vacuo to leave a residue. Flash chromatography over silica, eluting with ethyl acetate:heptane mixtures 0:100 to 65:35 gave alcohol (18) (11.58 g, 80%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039641B2
Source datasetuspto-grants-2011_10
ORD IDord-0fb4397a4f9e487789d3d9acf09b1c97
Source noteuspto-grants-2011_10